ClinVar Miner

Submissions for variant NM_000466.3(PEX1):c.2584-21_2584-20dup

dbSNP: rs5885806
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001509939 SCV001716855 benign Zellweger spectrum disorders 2024-03-04 criteria provided, single submitter clinical testing

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